Please choose an event type to view the corresponding MedsFacts report:

FEBRILE NEUTROPENIA ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
APPLICATION SITE REACTION ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
BACTERAEMIA ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
MUCORMYCOSIS ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FALL ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)

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